MOLT PERIOSTEAL ELEVATOR 1103-583

GUDID 00192896053229

MOLT PERIOSTEAL ELEVATOR #CS M-9

SONTEC INSTRUMENTS, INC.

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• Primary Device ID: 00192896053229
• NIH Device Record Key: ac4606bf-3813-4967-aa9b-b9ee955c546b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MOLT PERIOSTEAL ELEVATOR
• Version Model Number: 1103-583
• Catalog Number: 1103-583
• Company DUNS: 040729840
• Company Name: SONTEC INSTRUMENTS, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800) 821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800) 821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800) 821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800) 821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800) 821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800) 821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800) 821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800) 821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800) 821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800) 821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800) 821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800) 821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800) 821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800) 821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800) 821-7496
• Email: info@sontecinstruments.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896053229 [Primary]

FDA Product Code

• EMJ: ELEVATOR, SURGICAL, DENTAL

Sterilization

• Steralize Prior To Use: true
• Device Is Sterile: false

[00192896053229]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896053229]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896053229]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896053229]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896053229]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896053229]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896053229]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896053229]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896053229]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896053229]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896053229]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896053229]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896053229]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896053229]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896053229]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2019-06-27
• Device Publish Date: 2018-09-24

On-Brand Devices [MOLT PERIOSTEAL ELEVATOR]

• 00192896082908: MOLT PERIOSTEAL ELEVATOR SINGLE ENDED TIP #EX-6
• 00192896053229: MOLT PERIOSTEAL ELEVATOR #CS M-9
• 00192896052819: MOLT PERIOSTEAL ELEVATOR #MX2/4 DOUBLE ENDED BLADE
• 00192896093928: MOLT PERIOSTEAL ELEVATOR DOUBLE ENDED TIPS #EX-1